首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   16080篇
  免费   1371篇
  国内免费   1964篇
  19415篇
  2024年   53篇
  2023年   285篇
  2022年   600篇
  2021年   939篇
  2020年   709篇
  2019年   833篇
  2018年   775篇
  2017年   568篇
  2016年   737篇
  2015年   1073篇
  2014年   1285篇
  2013年   1314篇
  2012年   1610篇
  2011年   1484篇
  2010年   922篇
  2009年   750篇
  2008年   835篇
  2007年   781篇
  2006年   627篇
  2005年   539篇
  2004年   401篇
  2003年   315篇
  2002年   294篇
  2001年   196篇
  2000年   186篇
  1999年   179篇
  1998年   129篇
  1997年   121篇
  1996年   117篇
  1995年   104篇
  1994年   92篇
  1993年   76篇
  1992年   91篇
  1991年   57篇
  1990年   60篇
  1989年   52篇
  1988年   36篇
  1987年   30篇
  1986年   29篇
  1985年   30篇
  1984年   15篇
  1983年   14篇
  1982年   13篇
  1981年   5篇
  1980年   4篇
  1979年   10篇
  1978年   4篇
  1976年   9篇
  1975年   8篇
  1971年   3篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
71.
CRISPR/Cas12a is a single effector nuclease that, like CRISPR/Cas9, has been harnessed for genome editing based on its ability to generate targeted DNA double strand breaks (DSBs). Unlike the blunt-ended DSB generated by Cas9, Cas12a generates sticky-ended DSB that could potentially aid precise genome editing, but this unique feature has thus far been underutilized. In the current study, we found that a short double-stranded DNA (dsDNA) repair template containing a sticky end that matched one of the Cas12a-generated DSB ends and a homologous arm sharing homology with the genomic region adjacent to the other end of the DSB enabled precise repair of the DSB and introduced a desired nucleotide substitution. We termed this strategy ‘Ligation-Assisted Homologous Recombination’ (LAHR). Compared to the single-stranded oligo deoxyribonucleotide (ssODN)-mediated homology directed repair (HDR), LAHR yields relatively high editing efficiency as demonstrated for both a reporter gene and endogenous genes. We found that both HDR and microhomology-mediated end joining (MMEJ) mechanisms are involved in the LAHR process. Our LAHR genome editing strategy, extends the repertoire of genome editing technologies and provides a broader understanding of the type and role of DNA repair mechanisms involved in genome editing.  相似文献   
72.
染色质是真核生物细胞核内由核酸和蛋白质组成的复合结构,有着精密且复杂的三维结构。染色质除基本的DNA序列外,内部还存在着不同化学修饰,DNA-蛋白质相互作用,DNA-DNA相互作用和DNA-RNA相互作用,以上这些若发生改变都可能在肿瘤发生发展过程中起到至关重要的作用。通过不同的染色质测序方法,可以解析出这些改变,并进一步加深研究者对肿瘤形成机制的理解,最终应用于肿瘤的治疗。本文对常见的染色质测序技术部分原理和应用进行综述。  相似文献   
73.
Mutations in VPS13C cause early-onset, autosomal recessive Parkinson’s disease (PD). We have established that VPS13C encodes a lipid transfer protein localized to contact sites between the ER and late endosomes/lysosomes. In the current study, we demonstrate that depleting VPS13C in HeLa cells causes an accumulation of lysosomes with an altered lipid profile, including an accumulation of di-22:6-BMP, a biomarker of the PD-associated leucine-rich repeat kinase 2 (LRRK2) G2019S mutation. In addition, the DNA-sensing cGAS-STING pathway, which was recently implicated in PD pathogenesis, is activated in these cells. This activation results from a combination of elevated mitochondrial DNA in the cytosol and a defect in the degradation of activated STING, a lysosome-dependent process. These results suggest a link between ER-lysosome lipid transfer and innate immune activation in a model human cell line and place VPS13C in pathways relevant to PD pathogenesis.  相似文献   
74.
新疆苦豆子根瘤菌的数值分类研究   总被引:8,自引:0,他引:8  
苦豆子(Sophora alopecuroides)对于干旱荒漠地区的畜牧业发展有着非常重要的意义,其生长特性与根瘤菌有密切关系。我们对分离自新疆苦豆子根瘤的67株根瘤菌及36个模式菌株进行了118项表型性状的测定,包括唯一碳源利用、唯一氮源利用、对抗生素和染料的抗性、耐盐性、初始pH值生长范围、生长温度范围及石蕊牛奶反应、氧化酶、过氧化氢酶和脲酶。对测定结果用聚类分析方法进行了分析,获得数值分类树状图。结果表明:新疆苦豆子根瘤菌在碳氮源利用、抗生素敏感性以及对染料的抗性程度等方面存在着差异。新疆苦豆子根瘤菌能耐受低温,并具有较强的耐盐、碱能力,所有供试菌株均能在初始pH值为9-12的YMA培养基上生长,92.5%的菌株能耐受3.0%的NaCl,91.0%的菌株能耐受4.0%的NaCl,有18株菌甚至能耐受5.0%和6.0%的NaCl。聚类结果表明, 在84.8%的相似性水平上,67个供试菌株构成了4个新的表观群,第Ⅰ、Ⅱ、Ⅲ、Ⅳ类群分别有21、7、4、3个菌株,中心菌株分别为NWBC152、NWTKX101、NWYJS12、NWLP112。此外,数值分类结果还表明,苦豆子根瘤菌与模式菌株的相似性较低,它们所形成的4个独立群可能有新种出现。  相似文献   
75.
This paper reports the ways that the differences in leaf senescence are related to grain filling, grain yield, and the dynamics of cytokinins (CKs) in the top three leaves of four field-grown new plant type (NPT) rice, a tropical japonica developed at the International Rice Research Institute, Philippines, to increase the yield potential of rice. The chlorophyll content in leaves decreased from flowering to maturity in all the NPT lines, whereas the grain filling percentage was higher in the fast-senescing NPT line than in slow-senescing NPT line. Grain yield was positively correlated with senescence in the flag leaf. Rapid changes in the CK levels were recorded in the leaves of the fast-senescing line, whereas the CK levels were relatively stable in leaves of the slow-senescing line, suggesting that the dynamics of CKs in the fast-senescing line are vital for fast senescence. There were no significant changes in bioactive CKs, CK O-glucosides (storage CKs), and cis-zeatin derivatives in different leaves of the slow-senescing NPT line between 0 and 3 weeks after flowering, suggesting that the content of these CKs is relatively stable during grain filling. A progressive increase in levels of bioactive CKs was positively correlated with gradual accumulation of CK N-glucosides (inactive CKs) in the top three leaves of the slow-senescing NPT line, whereas the decrease of bioactive CKs in the flag leaf of the fast-senescing line was accompanied by accumulation of CK O-glucosides. These results suggest that there is a higher rate of biosynthesis and/or import of bioactive CKs as well as their turnover which may favor delay of leaf senescence in the slow-senescing NPT line.  相似文献   
76.
柴强  黄高宝  黄鹏 《应用生态学报》2006,17(9):1624-1628
通过盆栽试验,探讨供水(田间持水量的45%、60%和75%)和化感物质间甲酚对小麦、蚕豆不同种植模式生长盛期土壤微生物多样性和酶活性的影响.结果表明,随灌水水平的降低,不同处理的土壤细菌、真菌和放线菌数量随之减少,间甲酚可加剧灌水减少引起的微生物数量的减少;间甲酚对不同处理土壤微生物多样性指数均具有降低作用,提高灌水水平可缓解间甲酚对间作群体土壤微生物多样性的负效应,但间甲酚在75%灌水水平下对单作微生物多样性的负效应最大,45%的供水水平和间甲酚作用下间作可维持更高的土壤微生物多样性.间甲酚对土壤过氧化氢酶的化感作用不显著,对脲酶和酸性磷酸酶活性的化感作用显著;3种土壤酶活性随供水水平的降低均显著下降,但供水与间甲酚、种植模式的互作效应对酶活性的影响不显著;间作对土壤过氧化氢酶和酸性磷酸酶活性具有极显著影响.  相似文献   
77.
农田土壤紧实的发生、影响及其改良   总被引:14,自引:0,他引:14  
土壤紧实是影响农田土壤质量和作物生长的关键障碍因子之一,是当前土壤功能及农田生态健康研究领域的重点。本文分析了近年来国内外关于土壤紧实的发生原因、影响因素、改良措施的研究进展。除农业机械以外,耕作制度和水肥管理对紧实的影响也不可忽视,此外,各因素的影响程度会随时空而变化。在综合分析已有研究的基础上,就目前土壤紧实研究中亟待解决的问题进行了探讨,认为今后应加强以下几方面的研究:1)从分子方面探讨抗紧实作物的遗传机理;2)田间可视化评价结合模型研究紧实下土壤-作物的变化过程;3)深入探讨土壤紧实的改良措施,为今后农田健康的相关研究提供参考。  相似文献   
78.
目的建立针对Nipah病毒N基因的一步法Real-time RT-PCR检测方法,用于Nipah病毒感染样本的快速准确检测和定量。方法针对Nipah病毒的保守基因N设计引物和探针,建立一步法Real-time RT-PCR反应方法并分析敏感性和特异性。结果所设计的引物经Blast检索可以用于检测所有已知的Nipah病毒株。本研究建立的一步法Real-time RT-PCR方法可以特异性检测出Nipah病毒,不与Hendra病毒产生交叉反应。检测灵敏度为1.1×100~1.1×101copies/μl。标准曲线的线性范围为1.1×102~1.1×106copies/μl。结论本研究建立的一步法real-time RT-PCR方法敏感性和特异性较高,且不易出现污染引起的假阳性结果,适合用于Nipah病毒感染样本的检测。  相似文献   
79.
Lipoxygenases (LOXs) are enzymes involved in lipid peroxidation. Here we reported the identification, molecular and functional characterization of the gene encoding rice (Oryza sativa L.) seed LOX3 (sLOX3). Via a map-based cloning strategy we identified Os03g0700400 as the candidate gene encoding sLOX3. Further functional complementary test and biochemical characterization of the recombinant Os03g0700400 protein verified the identification. The sLOX3 gene was highly expressed in roots, moderately in embryos and very weakly in leaves, leaf sheaths and stems. Transient expression experiment (in rice protoplasts) and subsequent laser confocal microscopic analysis demonstrated that the sLOX3 protein was localized into the cytosol. We next showed that overexpression of sLOX3 in a japonica sLOX3-normal rice cultivar, Wuyunjing 7 accelerated the decrease of seed germination ability when the seeds were routinely stored, which demonstrated that sLOX3 had a negative effect on seed longevity (storability). Meanwhile, an increased occurrence of embryo decay was observed in the same transgenic seeds, suggesting that sLOX3 might negatively affect seed longevity by facilitating colonization of particular seed pathogens. Our result forwarded the understanding of the effects of 9-LOX on rice seed longevity.  相似文献   
80.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号